Literature DB >> 19009218

Testing pulmonary vasoreactivity.

Edmundo Clarindo Oliveira1, Carlos Faria Santos Amaral, Marco Antonio Moura, Frederico Thadeu Assis Figueiredo Campos, Helder Machado Pauperio.   

Abstract

Pulmonary arterial hypertension is classified as idiopathic or secondary (associated with collagenoses, heart disease, portal hypertension, pulmonary thromboembolism, and pulmonary vascular diseases). Pulmonary vasoreactivity should be tested in order to define the best treatment option. Of the many drugs that have been used to test pulmonary vasoreactivity, inhaled nitric oxide is the best choice, due its specific pulmonary effect and very short half-life (5-10 s). The results of this test identify candidates for heart surgery among patients with congenital heart disease and candidates for the use of calcium antagonists among patients with other forms of pulmonary hypertension. Performing and interpreting the results of such tests are a great responsibility, since mistakes can lead to incorrect treatment decisions, resulting in the death of patients.

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Year:  2008        PMID: 19009218     DOI: 10.1590/s1806-37132008001000013

Source DB:  PubMed          Journal:  J Bras Pneumol        ISSN: 1806-3713            Impact factor:   2.624


  3 in total

1.  Acute vasoreactivity test results in severe pulmonary hypertension patients with chronic obstructive pulmonary disease: our experience with 29 cases.

Authors:  Selvi Asker; Muntecep Asker
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2015-05-28

2.  Large Atrial Septal Defect Closure in a Patient with Severe Pulmonary Arterial Hypertension.

Authors:  Supomo Supomo; Anggoro Budi Hartopo; Dyah Wulan Anggrahini; Handy Darmawan; Lucia Kris Dinarti
Journal:  Korean J Thorac Cardiovasc Surg       Date:  2017-10-05

3.  Congenital Supravalvar Mitral Ring - A Case Report.

Authors:  Raquel Reis Soares; Leonardo Ferber; Matheus Ferber; Daniel Soares Mata
Journal:  Braz J Cardiovasc Surg       Date:  2020-02-01
  3 in total

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